Exploring the Steric Hindrance of Alkylammonium Cations in the Structural Reconfiguration of Quasi-2D Perovskite Materials Using a High-throughput Experimental Platform

作者:Zhang, Jiyun*; Wu, Jianchang; Langner, Stefan; Zhao, Baolin; Xie, Zhiqiang; Hauch, Jens A.; Afify, Hany A.; Barabash, Anastasia; Luo, Junsheng; Sytnyk, Mykhailo; Meng, Wei; Zhang, Kaicheng; Liu, Chao; Osvet, Andres; Li, Ning; Halik, Marcus; Heiss, Wolfgang; Zhao, Yicheng*; Brabec, Christoph J.*
来源:Advanced Functional Materials, 2022, 32(43): 2207101.
DOI:10.1002/adfm.202207101

摘要

Reduced-dimensional (2D or quasi-2D) perovskites have recently attracted considerable interest due to their superior long-term stability. The nature of the intercalating cations plays a key role in determining the physicochemical properties and stability of the quasi-2D perovskites. Here, the thermal stability of a series of 2D Ruddlesden-Popper (RP) perovskites is studied using seven types of intercalating cations with increasing linear carbon-chain length from ethylammonium (EA) to n-dodecylammonium (DA) through a high-throughput platform. The results show that long-chain cations in quasi-2D perovskite films lead to strong steric hindrance between adjacent perovskite domains, thus suppressing Ostwald ripening during the thermal-aging process. For short-chain cations, increased-dimensional phase redistribution during the aging period is observed, which can benefit a concomitant regeneration of the 3D/3D-like perovskite phases. The impact of steric hindrance on structural reconfiguration and the subsequent phase redistribution in quasi-2D perovskites are systematically characterized by UV-vis absorption spectra, photoluminescence spectra, and X-ray diffraction patterns. Due to the steric hindrance effect, an optimal chain length is found to maximize film stability by balancing the water/oxygen resistance and increased-dimensional phase redistribution. This work provides new insight into the thermal stability of quasi-2D perovskites.

  • 单位
    i; 电子科技大学